Soleno Therapeutics, Inc. (SLNO) Stock Analysis
Healthcare · Biotechnology
Hold if already holding. Not a fresh buy at $53.02, but acceptable to hold if already in. Reasons: Concentration risk — Product: VYKAT XR; Analyst target reached - limited upside remaining.
Soleno Therapeutics received FDA approval on March 26, 2025 for VYKAT XR (diazoxide choline extended-release), the first approved treatment for hyperphagia in Prader-Willi syndrome patients age 4+. Revenue began in Q2 2025 from VYKAT XR sales; the company had net income of... Read more
Hold if already holding. Not a fresh buy at $53.02, but acceptable to hold if already in. Reasons: Concentration risk — Product: VYKAT XR; Analyst target reached - limited upside remaining. Chart setup: No recognized chart pattern (not a breakout, bounce, continuation, recovery, falling knife, or range) — technicals mixed. News gate: 0 distinct critical events (0 MATERIAL_RISK articles) Score 5.2/10, moderate confidence.
Passes 8/10 gates (positive momentum, clean insider activity, positive momentum, no SEC red flags, news events none recent, earnings proximity 77d clear, semi cycle peak clear, materials cycle peak clear). Fails on favorable risk/reward ratio. Suitability: aggressive.
Recent Developments — Soleno Therapeutics, Inc.
Latest news
- SHAREHOLDER ALERT Securities Class Action Filed Against Soleno Therapeutics, Inc. (SLNO) - TMX Newsfile — TMX Newsfile negative
- Soleno Therapeutics (SLNO) Projected to Post Earnings on Wednesday - MarketBeat — MarketBeat neutral
- Soleno Therapeutics, Inc. Class Action Reminder - Robbins LLP Enc - The National Law Review — The National Law Review negative
- SLNO DEADLINE ALERT: Hagens Berman Alerts Soleno Therapeutics (SLNO) Investors to Today's Lead Plaintiff Deadline in Sec — Morningstar negative
- SLNO INVESTOR NOTICE: Faruqi & Faruqi, LLP Reminds Soleno Therapeutics (SLNO) Investors of Securities Class Action Deadl — Morningstar negative
Generated 2026-05-20T21:06:21Z.
Thesis
Key Metrics
Quality Signals
Options Flow
Concentration Risks(10-K Item 1A)
- HIGHProductVYKAT XR10-K Item 1A: 'we have just begun to generate product revenue and are dependent upon the success of VYKAT XR'
Material Events(8-K, last 90d)
- 2026-02-26Item 5.02LOWJennifer Fulk appointed CFO effective March 2, 2026, succeeding James Mackaness who intends to retire by end of March. Fulk was previously CFO of 120Water Inc. and Talkspace, Inc. Planned succession; no disagreement cited.SEC filing →
Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results. Full disclaimer
Rating Breakdown
2 floor-breakers·1 ceiling hit
Technicals below the gate floor. Component breakdown shows what dragged the score down.static
Priced at a premium — multiples above sector norms. Needs delivery on growth + margins to justify.static
Price Targets
Position Sizing
Risk Alerts
Earnings
Verdict History
Frequently Asked Questions
Hold if already holding. Not a fresh buy at $53.02, but acceptable to hold if already in. Reasons: Concentration risk — Product: VYKAT XR; Analyst target reached - limited upside remaining. Chart setup: No recognized chart pattern (not a breakout, bounce, continuation, recovery, falling knife, or range) — technicals mixed. News gate: 0 distinct critical events (0 MATERIAL_RISK articles) Target $60.96 (+15.0%), stop $52.83 (−0.4%), A.R:R -0.9:1. Score 5.2/10, moderate confidence.
Take-profit target: $60.96 (+15.1% upside). Target $60.96 (+15.0%), stop $52.83 (−0.4%), A.R:R -0.9:1. Stop-loss: $52.83.
Concentration risk — Product: VYKAT XR; Analyst target reached - limited upside remaining; Earnings estimates trending DOWN.
Soleno Therapeutics, Inc. trades at a P/E of 27.5 (forward -23.4). TrendMatrix value score: 2.9/10. Verdict: Hold.
16 analysts cover SLNO with a consensus score of 2.7/5. Average price target: $53.
What does Soleno Therapeutics, Inc. do?Soleno Therapeutics received FDA approval on March 26, 2025 for VYKAT XR (diazoxide choline extended-release), the...
Soleno Therapeutics received FDA approval on March 26, 2025 for VYKAT XR (diazoxide choline extended-release), the first approved treatment for hyperphagia in Prader-Willi syndrome patients age 4+. Revenue began in Q2 2025 from VYKAT XR sales; the company had net income of $20.9M in 2025 but an accumulated deficit of $431.4M from prior clinical-stage losses.